A simple fluorescent strategy for liver capillary labeling with carbon quantum dot-lectin nanoprobe

Taking the hepatic sinusoid (HS) as the main delivery area of liver nutrients and metabolic waste, recognizing its structure is important for a deep understanding of liver function. In this paper, based on lycopersicon esculentum lectin (LEL), with targeting ability for endothelial cells, and carbon...

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Veröffentlicht in:Analyst (London) 2022-05, Vol.147 (9), p.1952-196
Hauptverfasser: An, Chang-Zhi, Li, Chao-Qing, Song, Lai-Bo, He, Yan-Fei, Chen, Wei, Liu, Bo, Zhao, Yuan-Di
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container_start_page 1952
container_title Analyst (London)
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creator An, Chang-Zhi
Li, Chao-Qing
Song, Lai-Bo
He, Yan-Fei
Chen, Wei
Liu, Bo
Zhao, Yuan-Di
description Taking the hepatic sinusoid (HS) as the main delivery area of liver nutrients and metabolic waste, recognizing its structure is important for a deep understanding of liver function. In this paper, based on lycopersicon esculentum lectin (LEL), with targeting ability for endothelial cells, and carbon quantum dots (CQDs), with high biosafety, an LEL-coupled CQD immunofluorescence probe (CQD@LEL) that can label microvessels is designed and used for the fluorescence labeling and imaging of HS in liver tissue sections. The CQD size is approximately 2 nm. Blue fluorescence is emitted under excitation; its optimal excitation wavelength is 400 nm while the emission is at about 450 nm. Gel electrophoresis and capillary electrophoresis confirm that glutaraldehyde can couple LEL to CQD, and the obtained CQD@LEL retains the fluorescence property and has good stability. Optimization experiments show that its labeling effect is positively correlated with time and probe concentration for dyeing the blood vessels of mouse liver slices. In order to improve the effect further, a probe concentration of 0.17 mg mL −1 and incubation time of 3 h were chosen to label the liver tissue sections. The results show that the liver microvessels are formed by interstitial structures among the hepatic cords, and the HS presents a granular or patchy appearance. H&E and ultrathin section TEM show that the microvascular wall of the liver is composed of discontinuous endothelial cells, and there are Kupffer cells and other cells in the tubes, proving that our probe can clearly label the structure and morphology of liver microvessels. This work is of great significance for the visualization of HS. Based on lycopersicon esculentum lectin that can target vascular endothelial cells and carbon quantum dots, we designed a carbon-based probe for the fluorescence labeling and imaging of hepatic blood vessels of liver tissue sections.
doi_str_mv 10.1039/d1an02364k
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In this paper, based on lycopersicon esculentum lectin (LEL), with targeting ability for endothelial cells, and carbon quantum dots (CQDs), with high biosafety, an LEL-coupled CQD immunofluorescence probe (CQD@LEL) that can label microvessels is designed and used for the fluorescence labeling and imaging of HS in liver tissue sections. The CQD size is approximately 2 nm. Blue fluorescence is emitted under excitation; its optimal excitation wavelength is 400 nm while the emission is at about 450 nm. Gel electrophoresis and capillary electrophoresis confirm that glutaraldehyde can couple LEL to CQD, and the obtained CQD@LEL retains the fluorescence property and has good stability. Optimization experiments show that its labeling effect is positively correlated with time and probe concentration for dyeing the blood vessels of mouse liver slices. In order to improve the effect further, a probe concentration of 0.17 mg mL −1 and incubation time of 3 h were chosen to label the liver tissue sections. The results show that the liver microvessels are formed by interstitial structures among the hepatic cords, and the HS presents a granular or patchy appearance. H&amp;E and ultrathin section TEM show that the microvascular wall of the liver is composed of discontinuous endothelial cells, and there are Kupffer cells and other cells in the tubes, proving that our probe can clearly label the structure and morphology of liver microvessels. This work is of great significance for the visualization of HS. 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In order to improve the effect further, a probe concentration of 0.17 mg mL −1 and incubation time of 3 h were chosen to label the liver tissue sections. The results show that the liver microvessels are formed by interstitial structures among the hepatic cords, and the HS presents a granular or patchy appearance. H&amp;E and ultrathin section TEM show that the microvascular wall of the liver is composed of discontinuous endothelial cells, and there are Kupffer cells and other cells in the tubes, proving that our probe can clearly label the structure and morphology of liver microvessels. This work is of great significance for the visualization of HS. Based on lycopersicon esculentum lectin that can target vascular endothelial cells and carbon quantum dots, we designed a carbon-based probe for the fluorescence labeling and imaging of hepatic blood vessels of liver tissue sections.</description><subject>Animals</subject><subject>Blood vessels</subject><subject>Capillaries</subject><subject>Carbon</subject><subject>Carbon - chemistry</subject><subject>Coloring Agents</subject><subject>Cords</subject><subject>Electrophoresis</subject><subject>Endothelial Cells</subject><subject>Excitation</subject><subject>Fluorescence</subject><subject>Immunofluorescence</subject><subject>Labeling</subject><subject>Lectins</subject><subject>Liver</subject><subject>Metabolic wastes</subject><subject>Mice</subject><subject>Nutrients</subject><subject>Optimization</subject><subject>Quantum dots</subject><subject>Quantum Dots - chemistry</subject><subject>Tubes</subject><issn>0003-2654</issn><issn>1364-5528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1PwzAMhiMEYmNw4Q6KxAUhFfLVNj1O41NMcIFzlabp6EiTLUlB-_cENobEybL9yH79GoBjjC4xosVVjYVBhGbsfQcMcYxJmhK-C4YIIZqQLGUDcOD9PKYYpWgfDGjKEM0oGgI5hr7tFlrBRvfWKS-VCdAHJ4KarWBjHdTth3JQikWrtXArqEWldGtm8LMNb7HuKmvgshcm9B2sbUi0kqE10AhjF85W6hDsNUJ7dbSJI_B6e_MyuU-mz3cPk_E0kZTmIakxRVJyjglhUhBSFQ1VFKVZLRnJhGy4qFWd1wxVrJA8p43iuKlwHjucFISOwPl6bty67JUPZdfGe6Jqo2zvS5KxgqQoY3lEz_6hc9s7E9VFKuV5zjPMI3WxpqSz3jvVlAvXdtGDEqPy2_ryGo-ffqx_jPDpZmRfdareor9eR-BkDTgvt92_39EvSnSJKg</recordid><startdate>20220503</startdate><enddate>20220503</enddate><creator>An, Chang-Zhi</creator><creator>Li, Chao-Qing</creator><creator>Song, Lai-Bo</creator><creator>He, Yan-Fei</creator><creator>Chen, Wei</creator><creator>Liu, Bo</creator><creator>Zhao, Yuan-Di</creator><general>Royal Society of Chemistry</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8634-7608</orcidid><orcidid>https://orcid.org/0000-0002-5450-5528</orcidid><orcidid>https://orcid.org/0000-0002-4286-4275</orcidid></search><sort><creationdate>20220503</creationdate><title>A simple fluorescent strategy for liver capillary labeling with carbon quantum dot-lectin nanoprobe</title><author>An, Chang-Zhi ; 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source MEDLINE; Royal Society of Chemistry Journals Archive (1841-2007); Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Animals
Blood vessels
Capillaries
Carbon
Carbon - chemistry
Coloring Agents
Cords
Electrophoresis
Endothelial Cells
Excitation
Fluorescence
Immunofluorescence
Labeling
Lectins
Liver
Metabolic wastes
Mice
Nutrients
Optimization
Quantum dots
Quantum Dots - chemistry
Tubes
title A simple fluorescent strategy for liver capillary labeling with carbon quantum dot-lectin nanoprobe
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